Veterinary medicinal product register

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Data selected by 1069
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Milprazon 4 mg/10 mg - V/DCP/15/0009 KRKA, d.d., Novo mesto, Slovēnija QP54AB51 small cats; kittens weighing at least 0.5 kg Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Milbemycin oxime, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 26-Feb-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Apr-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Apr-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-Apr-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0009-01 1 Al/OPA/Al/PVH blisteris, 2 tablete [JPG] [JPG]
V/DCP/15/0009-02 1 Al/OPA/Al/PVH blisteris, 4 tablete [PDF]
V/DCP/15/0009-03 12 Al/OPA/Al/PVH blisteris, 4 tablete [PDF]
Forthyron flavour 800 µg/tabl. V/MRP/18/0052 Eurovet Animal Health B.V., Nīderlande QH03AA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Levothyroxine sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande;Dales Pharmaceuticals Ltd., Lielbritānija;GENERA Inc., Horvātija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 260122LI (26-Jan-2022)
Labelling text: [DOCX] 20112020M (20-Nov-2020)
Summary of product characteristics: [DOCX] 20112020ZA (20-Nov-2020)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/18/0052-01 50 alumīnija/PVC/PE/PVDC blisteris, 10 tablete [PDF]
V/MRP/18/0052-02 250 alumīnija/PVC/PE/PVDC blisteris, 10 tablete [PDF] [PDF]
LV Intrafer-200 B12 - V/NRP/20/0034 Interchemie Werken De Adelaar Eesti AS, Igaunija QB03AE cattle; pigs; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Iron(III)-hydroxide dextran complex, Cyanocobalamin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Interchemie Werken De Adelaar Eesti AS, Igaunija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 30062020LI (30-Jun-2020)
Labelling text: [DOCX] 30062020M (30-Jun-2020)
Summary of product characteristics: [DOCX] 30062020ZA (30-Jun-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/20/0034-01 1 Stikla flakons, 100 ml -
LV Biocillin-200 WS 200 mg/g V/NRP/11/0064 Interchemie Werken De Adelaar Eesti AS, Igaunija QJ01CA04 poultry; pigs Vairāk

Medicinal product information

Pharmaceutical form: powder for oral solution
International name (active substance): Amoxicillin trihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Interchemie Werken De Adelaar Eesti AS, Igaunija
Date of authorisation/renewal: 30-Nov-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 281116LI (30-Nov-2016)
Labelling text: [PDF] 281116M (30-Nov-2016)
Summary of product characteristics: [PDF] 281116ZA (30-Nov-2016)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/11/0064-01 200 mg/g 1 ABPE trauciņš, 1000 g [JPG]
Tialin 250 mg/ml V/DCP/18/0032 Dechra Regulatory B.V., Nīderlande QJ01XQ01 pigs; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for use in drinking water
International name (active substance): Tiamulin hydrogen fumarate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande;GENERA Inc., Horvātija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Aug-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Aug-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-Aug-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0032-01 1 ABPE pudele, 1 l -
V/DCP/18/0032-02 1 Polietilēna konteiners, 5 l -
Prednicortone vet 20 mg V/DCP/15/0025 Dechra Regulatory B.V., Nīderlande QH02AB06 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Prednisolone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 30-Jun-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0025-01 20 mg 1 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-02 20 mg 2 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-03 20 mg 3 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-04 20 mg 4 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-05 20 mg 5 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-06 20 mg 6 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-07 20 mg 7 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-08 20 mg 8 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-09 20 mg 9 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-10 20 mg 10 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-11 20 mg 15 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-12 20 mg 25 Al/PE blisteris, 10 tablete -
V/DCP/15/0025-13 20 mg 50 Al/PE blisteris, 10 tablete -
Prednicortone vet 5 mg V/DCP/15/0024 Dechra Regulatory B.V., Nīderlande QH02AB06 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Prednisolone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 30-Jun-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0024-01 5 mg 1 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-02 5 mg 2 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-03 5 mg 3 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-04 5 mg 4 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-05 5 mg 5 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-06 5 mg 6 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-07 5 mg 7 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-08 5 mg 8 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-09 5 mg 9 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-10 5 mg 10 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-11 5 mg 15 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-12 5 mg 25 PVH/PVdH/Al blisteris, 10 tablete -
V/DCP/15/0024-13 5 mg 50 PVH/PVdH/Al blisteris, 10 tablete -
Clindacutin 10 mg/g V/DCP/21/0008 Dechra Regulatory B.V., Nīderlande QD06AX dogs Vairāk

Medicinal product information

Pharmaceutical form: ointment
International name (active substance): Clindamycin (as Clindamycin hydrochloride)
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0008-01 10 mg/g 1 Alumīnija tūbiņa, 20 g -
Amoxyvet 697 mg/g V/DCP/22/0035 Huvepharma NV, Beļģija QJ01CA04 pigs; chickens Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water
International name (active substance): Amoxicillin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release HUVEPHARMA SA, Francija
Date of authorisation/renewal: 27-Jul-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Sep-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Sep-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Sep-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0035-01 697 mg/g 1 Burciņa, 100 g -
V/DCP/22/0035-02 697 mg/g 1 Polietilēna maiss, 100 g -
V/DCP/22/0035-03 697 mg/g 1 Polietilēna maiss, 500 g -
V/DCP/22/0035-04 697 mg/g 1 Polietilēna maiss, 1 kg -
Dozuril 25 mg/ml V/DCP/12/0036 Dopharma Research B.V., Nīderlande QP51AJ01 chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for use in drinking water
International name (active substance): Toltrazuril
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 04-Jul-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOC] 200421MLI (20-Apr-2021)
Labelling text: [DOC] 200421MLI (20-Apr-2021)
Summary of product characteristics: [DOC] 200421ZA (20-Apr-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0036-01 25 mg/ml 1 Polietilēna pudelīte, 1 l -
V/DCP/12/0036-02 25 mg/ml 1 Polietilēna pudelīte, 5 l -
Parofor crypto 140000 IU/ml V/DCP/19/0046 Huvepharma NV, Beļģija QA07AA06 sheep; goats Vairāk

Medicinal product information

Pharmaceutical form: solution for oral use
International name (active substance): Paromomycin sulfate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet Joint Stock Company., Bulgārija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Mar-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Mar-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (15-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0046-01 140000 IU/ml 1 ABPE pudele, 125 ml -
V/DCP/19/0046-02 140000 IU/ml 1 ABPE pudele, 250 ml -
V/DCP/19/0046-03 140000 IU/ml 1 ABPE pudele, 500 ml -
V/DCP/19/0046-04 140000 IU/ml 1 ABPE pudele, 1 l -
Huvecin 25 mg/ml V/DCP/22/0047 Huvepharma NV, Beļģija QJ01FA94 pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tulathromycin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet JSC, Bulgārija
Date of authorisation/renewal: 30-Nov-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jan-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jan-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Jan-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0047-01 25 mg/ml 1 Stikla pudele, 50 ml -
V/DCP/22/0047-02 25 mg/ml 1 Stikla pudele, 100 ml -
V/DCP/22/0047-03 25 mg/ml 1 Stikla pudele, 250 ml -
Huvecin 100 mg/ml V/DCP/22/0048 Huvepharma NV, Beļģija QJ01FA94 cattle; pigs; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tulathromycin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet JSC, Bulgārija
Date of authorisation/renewal: 30-Nov-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jan-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jan-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Jan-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0048-01 100 mg/ml 1 Stikla pudele, 20 ml -
V/DCP/22/0048-02 100 mg/ml 1 Stikla pudele, 50 ml -
V/DCP/22/0048-03 100 mg/ml 1 Stikla pudele, 100 ml -
V/DCP/22/0048-04 100 mg/ml 1 Stikla pudele, 250 ml -
Cefabactin vet 50 mg V/DCP/16/0015 Le Vet Beheer B.V., Nīderlande QJ01DB01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Cefalexin monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-Oct-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0015-01 50 mg 1 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-02 50 mg 2 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-03 50 mg 3 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-04 50 mg 4 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-05 50 mg 5 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-06 50 mg 6 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-07 50 mg 7 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-08 50 mg 8 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-09 50 mg 9 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-10 50 mg 10 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-11 50 mg 25 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0015-12 50 mg 10 Kastīte ar blisteri, 10 tablete -
Cefabactin vet 250 mg V/DCP/16/0016 Le Vet Beheer B.V., Nīderlande QJ01DB01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Cefalexin monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-Oct-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0016-01 250 mg 1 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-02 250 mg 2 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-03 250 mg 3 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-04 250 mg 4 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-05 250 mg 5 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-06 250 mg 6 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-07 250 mg 7 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-08 250 mg 8 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-09 250 mg 9 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-10 250 mg 10 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-11 250 mg 25 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0016-12 250 mg 10 Kastīte ar blisteri, 10 tablete -
Pigfen 40 mg/g V/DCP/16/0035 Huvepharma NV, Beļģija QP52AC13 pigs Vairāk

Medicinal product information

Pharmaceutical form: premix for medicated feeding stuff
International name (active substance): Fenbendazole
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, Bulgārija
Date of authorisation/renewal: 27-Oct-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Jan-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Jan-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Jan-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0035-01 40 mg/g 1 Polietilēna maiss, 1 kg -
V/DCP/16/0035-02 40 mg/g 1 Polietilēna maiss, 2 kg -
V/DCP/16/0035-03 40 mg/g 1 Polietilēna maiss, 5 kg -
V/DCP/16/0035-04 40 mg/g 1 Polietilēna maiss, 20 kg -
Hydrotrim 500 mg/g V/DCP/23/0050 Huvepharma NV, Beļģija QJ01EW10 pigs; sheep; chickens; pre-ruminant cattle Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water, milk or milk replacer
International name (active substance): Sulfadiazine sodium, Trimethoprim
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet JSC, Bulgārija
Date of authorisation/renewal: 18-Sep-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Sep-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Sep-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Sep-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/23/0050-01 1 Papīra/PE/Al folijas/PE paciņa, 100 g -
V/DCP/23/0050-02 1 Papīra/PE/Al folijas/PE paciņa, 1 kg -
Spotinor 10 mg/ml V/DCP/14/0048 Norbrook Laboratories (Ireland) Limited, Īrija QP53AC11 cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Deltamethrin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 30-Oct-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0048-01 10 mg/ml 1 ABPE pudele, 250 ml -
V/DCP/14/0048-02 10 mg/ml 1 ABPE pudele, 500 ml -
V/DCP/14/0048-03 10 mg/ml 1 ABPE mugursomas tipa konteiners (balts), 1 l -
V/DCP/14/0048-04 10 mg/ml 1 ABPE mugursomas tipa konteiners (balts), 2,5 l -
V/DCP/14/0048-05 10 mg/ml 2 ABPE pudele, 500 ml -
Canishield 0.77 g V/DCP/18/0038 Beaphar B.V., Nīderlande QP53AC11 medium dogs; small dogs Vairāk

Medicinal product information

Pharmaceutical form: medicated collar
International name (active substance): Deltamethrin
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Beaphar BV, Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Jan-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Jan-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0038-01 1 Paciņa, 1 deva -
V/DCP/18/0038-02 2 Paciņa, 1 deva -
Canishield 1.04 g V/DCP/18/0039 Beaphar B.V., Nīderlande QP53AC11 large dogs Vairāk

Medicinal product information

Pharmaceutical form: medicated collar
International name (active substance): Deltamethrin
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Beaphar BV, Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Jan-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Jan-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0039-01 1 Paciņa, 1 deva -
V/DCP/18/0039-02 2 Paciņa, 1 deva -

3081 record

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